Mental Retardation, X-Linked
"Mental Retardation, X-Linked" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or aberrations in the structure of the X chromosome (SEX CHROMOSOME ABERRATIONS).
| Descriptor ID |
D038901
|
| MeSH Number(s) |
C10.597.606.643.455 C16.320.322.500 C16.320.400.525
|
| Concept/Terms |
Mental Retardation, X-Linked- Mental Retardation, X-Linked
- Mental Retardation, X Linked
- Retardation, X-Linked Mental
- X-Linked Mental Retardations
- X-Linked Mental Retardation Disorders
- X Linked Mental Retardation Disorders
- X-Linked Mental Retardation Syndromes
- X Linked Mental Retardation Syndromes
- X-Linked Mental Retardation
- X Linked Mental Retardation
|
Below are MeSH descriptors whose meaning is more general than "Mental Retardation, X-Linked".
Below are MeSH descriptors whose meaning is more specific than "Mental Retardation, X-Linked".
This graph shows the total number of publications written about "Mental Retardation, X-Linked" by people in this website by year, and whether "Mental Retardation, X-Linked" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 2 | 0 | 2 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 2 | 0 | 2 |
| 2013 | 3 | 0 | 3 |
| 2014 | 1 | 0 | 1 |
| 2015 | 3 | 0 | 3 |
| 2018 | 2 | 1 | 3 |
| 2019 | 1 | 0 | 1 |
| 2020 | 3 | 1 | 4 |
| 2021 | 4 | 1 | 5 |
| 2022 | 2 | 2 | 4 |
| 2023 | 2 | 1 | 3 |
| 2024 | 3 | 1 | 4 |
| 2025 | 0 | 1 | 1 |
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Below are the most recent publications written about "Mental Retardation, X-Linked" by people in Profiles.
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ATRX silences Cartpt expression in osteoblastic cells during skeletal development. J Clin Invest. 2025 Jan 02; 135(1).
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Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression. Genome Med. 2024 Dec 18; 16(1):146.
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Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levels. Hum Mol Genet. 2024 11 08; 33(22):1986-2001.
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MED12 Loss-of-Function Variants as a Cause of Congenital Diaphragmatic Hernia in Females With Hardikar Syndrome and Nonspecific Intellectual Disability. Am J Med Genet A. 2025 Jan; 197(1):e63868.
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Development and validation of parent-reported gastrointestinal health scale in MECP2 duplication syndrome. Orphanet J Rare Dis. 2024 Feb 09; 19(1):52.
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Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study. J Neurodev Disord. 2023 10 13; 15(1):33.
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Deep phenotypic characterization of the retinal dystrophy in patients with RNU4ATAC-associated Roifman syndrome. Eye (Lond). 2023 12; 37(18):3734-3742.
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Exploring gastrointestinal health in MECP2 duplication syndrome. Neurogastroenterol Motil. 2023 08; 35(8):e14601.
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Context matters - Daxx and Atrx are not robust tumor suppressors in the murine endocrine pancreas. Dis Model Mech. 2022 08 01; 15(8).
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Increased Reliability of Visually-Evoked Activity in Area V1 of the MECP2-Duplication Mouse Model of Autism. J Neurosci. 2022 08 17; 42(33):6469-6482.